Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Imidazole → 2-(tert-butyldiphenylsilyloxy)-N-methylethanamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | 2-(Methylamino)ethanol | HCID 8016 | — |
| 반응물 | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(tert-butyldiphenylsilyloxy)-N-methylethanamine | HCID 11823158 | 31.1% |
반응 단계
To a solution of N-methylethanolamine (600 mg), in N,N-dimethylformamide were added imidazole (1.13 g) and tert-butyldiphenylsilyl chloride (2.20 g) at ambient temperature with stirring. After 8 hours, the mixture was diluted with water (60 ml) and was extracted with ethyl acetate (20 ml) twice. The organic layer was washed with water three times and brine, dried over magnesium sulfate. The solvent was removed in vacuo. The residue was purified by column chromatography eluting with dichloromethane-methanol to give N-(2-tert-butyldiphenylsilyloxyethyl)-N-methylamine (780 mg) as an oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06169095A |
| 출처 데이터셋 | uspto-grants-2001_01 |
| ORD ID | ord-12efae263eca4be991f2e94a41bf1af9 |
| 출처 메모 | uspto-grants-2001_01 |